BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    GAMMA RADIATION STERILIZATION PRECEDURE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FasTouch Absorbable Fixation System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DISP. FLUID ISOLATOR & PRESS. RELIEF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·April 30, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 21, 2007

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 10, 2012

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025